Completed NA INTERVENTIONAL 3-arm NCT03478241

Postoperative Pain Intensity Associated With the Use of Different Nickel Titanium Instrumentation Systems

Postoperative Pain Intensity Associated With the Use of Different Nickel Titanium Instrumentation Systems During Single-Appointment Non-Surgical Endodontic Retreatment: A Randomized Clinical Trial

Sponsor: Istanbul Medipol University Hospital

Conditions Endodontically Treated Teeth Pain, Postoperative

Interventions Group 1: single file rotary motion Group 2: multiple file rotary motion Group 3: single file reciprocal motion

Updated 5 times since 2018 Last updated: Mar 26, 2018 Started: Sep 30, 2016 Primary completion: Dec 31, 2016 Completion: Jan 31, 2017

This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

Listed as NCT03478241, this NA trial focuses on Endodontically Treated Teeth and Pain, Postoperative and remains completed. Sponsored by Istanbul Medipol University Hospital, it has been updated 5 times since 2016, reflecting limited change activity. This study adds to the evidence base for this therapeutic area through structured, versioned documentation.

Status Flow

Change History

5 versions recorded

Sep 2024 — Present [monthly]

Completed NA
Jul 2024 — Sep 2024 [monthly]

Completed NA
Jan 2021 — Jul 2024 [monthly]

Completed NA
Jun 2018 — Jan 2021 [monthly]

Completed NA
Apr 2018 — Jun 2018 [monthly]

Completed NA

First recorded

Sep 2016

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:

Istanbul Medipol University Hospital

Data source: Istanbul Medipol University Hospital

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations

No location information available.